Department of Medical, Oral and Biotechnological Sciences, University "G. d'Annunzio" of Chieti-Pescara, 66100 Chieti, Italy.
Department of Innovative Technologies in Medicine & Dentistry, University "G. d'Annunzio" of Chieti-Pescara, 66100 Chieti, Italy.
Oxid Med Cell Longev. 2021 Jan 19;2021:6679708. doi: 10.1155/2021/6679708. eCollection 2021.
Periodontitis is usually sustained from microorganism of oral cavity, like (). Periodontal disease is an infectious disease that afflicts a large number of people. Researches are investigating on the mesenchymal stem cells (MSCs) response to inflammatory events in combination with antioxidant substances. In particular, ascorbic acid (AA) increased cell proliferation, upregulated the cells pluripotency marker expression, provide a protection from inflammation, and induced the regeneration of periodontal ligament tissue. The purpose of the present research was to investigate the effects of AA in primary culture of human periodontal ligament stem cells (hPDLSCs) exposed to lipopolysaccharide (LPS-G). The effect of AA on hPDLSCs exposed to LPS-G was determined through the cell proliferation assay. The molecules involved in the inflammatory pathway and epigenetic regulation have been identified using immunofluorescence and Western blot analyses. miR-210 level was quantified by qRT-PCR, and the ROS generation was finally studied. Cells co-treated with LPS-G and AA showed a restoration in terms of cell proliferation. The expression of NFB, MyD88, and p300 was upregulated in LPS-G exposed cells, while the expression was attenuated in the co-treatment with AA. DNMT1 expression is attenuated in the cells exposed to the inflammatory stimulus. The level of miR-210 was reduced in stimulated cells, while the expression was evident in the hPDLSCs co-treated with LPS-G and AA. In conclusion, the AA could enhance a protective effect in periodontitis model, downregulating the inflammatory pathway and ROS generation and modulating the miR-210 level.
牙周炎通常由口腔中的微生物维持,如 (). 牙周病是一种影响大量人群的传染病。研究人员正在调查间充质干细胞(MSCs)对炎症事件的反应与抗氧化物质的结合。特别是抗坏血酸(AA)可增加细胞增殖,上调细胞多能性标志物的表达,提供炎症保护,并诱导牙周韧带组织再生。本研究旨在研究 AA 对脂多糖(LPS-G)暴露的原代培养人牙周膜干细胞(hPDLSCs)的影响。通过细胞增殖测定法确定 AA 对 LPS-G 暴露的 hPDLSCs 的影响。通过免疫荧光和 Western blot 分析鉴定了参与炎症途径和表观遗传调控的分子。通过 qRT-PCR 定量 miR-210 水平,并最终研究 ROS 的产生。与 LPS-G 和 AA 共同处理的细胞在细胞增殖方面表现出恢复。在 LPS-G 暴露的细胞中,NFB、MyD88 和 p300 的表达上调,而在 AA 共同处理时表达减弱。DNMT1 的表达在受到炎症刺激的细胞中减弱。刺激细胞中的 miR-210 水平降低,而在与 LPS-G 和 AA 共同处理的 hPDLSCs 中则表达明显。总之,AA 可以通过下调炎症途径和 ROS 的产生并调节 miR-210 水平来增强牙周炎模型的保护作用。
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